CN116425995B - Metal organic frame material, ligand and application thereof - Google Patents

Metal organic frame material, ligand and application thereof Download PDF

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CN116425995B
CN116425995B CN202310686547.0A CN202310686547A CN116425995B CN 116425995 B CN116425995 B CN 116425995B CN 202310686547 A CN202310686547 A CN 202310686547A CN 116425995 B CN116425995 B CN 116425995B
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metal organic
organic framework
ligand
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mof
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CN116425995A (en
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赵礼义
李衍初
张福松
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Jilin Zhuo Cai Xin Yan Technology Co ltd
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    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/26—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
    • G01N27/28—Electrolytic cell components
    • G01N27/30—Electrodes, e.g. test electrodes; Half-cells
    • G01N27/308—Electrodes, e.g. test electrodes; Half-cells at least partially made of carbon
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/22—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains four or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G83/00—Macromolecular compounds not provided for in groups C08G2/00 - C08G81/00
    • C08G83/008—Supramolecular polymers
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/26—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
    • G01N27/28—Electrolytic cell components
    • G01N27/30—Electrodes, e.g. test electrodes; Half-cells
    • G01N27/327—Biochemical electrodes, e.g. electrical or mechanical details for in vitro measurements
    • G01N27/3275—Sensing specific biomolecules, e.g. nucleic acid strands, based on an electrode surface reaction
    • G01N27/3278—Sensing specific biomolecules, e.g. nucleic acid strands, based on an electrode surface reaction involving nanosized elements, e.g. nanogaps or nanoparticles

Abstract

The invention discloses a metal organic framework material, a ligand thereof and application thereof, belonging to the technical field of biosensors. The invention prepares a ligand structure and applies the ligand structure to the synthesis of novel metal organic framework materials, the MOF materials can be used as raw materials for preparing PEC sensors, and the PEC sensors prepared by testing the metal organic framework materials have higher selectivity and high sensitivity to the detection of VEGF165, and the linear range is 10-1 multiplied by 10 8 fM, the lowest detection limit is 0.18. 0.18 fM. And the response current values of two interfering substances, namely alpha-fetoprotein (AFP) and carcinoembryonic antigen (CEA), only slightly change, so that the sensor material is the PEC sensor material with highest sensitivity and best anti-interference performance in the related report of VEGF165 detection.

Description

Metal organic frame material, ligand and application thereof
Technical Field
The invention relates to a metal organic framework material, a ligand thereof and application thereof, belonging to the technical field of biosensors.
Background
Angiogenesis of the tumor is required for growth, proliferation and metastasis of tumor cells, and vascular endothelial growth factor (Vascular endothelial growth factor, VEGF) is taken as a key regulator of angiogenesis, so that the occurrence and development of the tumor can be effectively reflected, and the aim of early screening of the tumor can be achieved by measuring the content of VEGF in serum. VEGF165, one of the subtypes of VEGF, is often overexpressed in cancer cells, affecting lymphangiogenesis and tumor metastasis, resulting in abnormally rapid growth and division of cancer cells. Therefore, the exploration of a highly accurate and sensitive VEGF165 detection method has important significance for clinical diagnosis of tumors. Common detection methods include an enzyme-linked immunosorbent assay, an immunohistochemical assay, a fluorescence spectrometry and the like, but the methods face the problems of high detection cost, complex operation and the like, and the photoelectrochemical biosensor has the advantages of low cost, rapid reading, simple operation and the like, so that the photoelectrochemical biosensor becomes a powerful candidate for VEGF165 detection.
Photoelectrochemical (PEC) biosensor is used as an emerging biomarker detection technology, inherits the unique property of the electrochemical biosensor, has the characteristic of completely separating an excitation source and a detection signal, and uses a light source as an excitation signal to achieve qualitative or quantitative analysis of an object to be detected by utilizing electron transfer between a semiconductor photoelectric material in an excited state and the object to be detected. However, the development of PEC sensors is limited due to the low sensitivity and poor interference immunity of the PEC sensors in the early stages. Therefore, it is necessary to develop PEC biosensors with higher sensitivity and higher anti-interference power.
Disclosure of Invention
The invention provides a metal organic framework material for a PEC sensor, which has excellent selectivity to VEGF165 and high sensitivity, and a ligand thereof, and aims to solve the problems of low sensitivity and poor anti-interference performance of the conventional PEC sensor.
The technical scheme of the invention is as follows:
one of the objects of the present invention is to provide a metal organic framework material, abbreviated as MOF-ET21, of the formula [ Nd (L) 2 ]Wherein L is C 88 H 82 N 8 O 8 。
The second object of the present invention is to provide a ligand for preparing the above metal organic framework material, the ligand having the structure:
。
it is a further object of the present invention to provide a use of the above metal-organic framework material, in particular for the preparation of PEC sensors.
Further defined, the application method is as follows:
the cDNA and aptamer were diluted to 2. Mu.M, stored at 90℃for 5 min, then gradually cooled to 37℃and finally the mixture incubated at 37℃for 2h to form dsDNA. Then sequentially ultrasonic cleaning the Glass Carbon Electrode (GCE) (5 cm ×0.4 cm) in acetone, ethanol and pure water for 15 min, and then usingBlowing nitrogen to dry; the effective area of the GCE electrode was then fixed with a fluorinated sealing tape at 0.16 cm 2 The method comprises the steps of carrying out a first treatment on the surface of the The MOF-ET21 dispersion was applied dropwise to the GCE electrode surface and dried 5 h in an electrically heated incubator at 37℃and then a mixed solution of 1-ethyl-3- (3-dimethylaminopropyl) -carbodiimide and N-hydroxysuccinimide (EDC/NHS) was applied dropwise to the MOF-ET21/GCE and activated 2h at 25 ℃. After EDC/NSH activation, dsDNA was coated on MOF-ET21/GCE and incubated at 25℃for 20 min, and the carboxyl groups of MOF-ET21/GCE reacted with the amino groups of dsDNA to form dsDNA/MOF-ET21/GCE. Then dsDNA/MOF-ET21/GCE was immersed in 0.25 wt% Bovine Serum Albumin (BSA) for 25 min to give a dsDNA/BSA/MOF-ET21/GCE structure, alkaline phosphatase (ALP) was added to the surface of dsDNA/BSA/MOF-ET21/GCE, and placed at 4℃for 2h, ALP-dsDNA/BSA/MOF-ET21/GCE was obtained by biotin-streptavidin system, and finally ALP-dsDNA/BSA/MOF-ET21/GCE was added to Tris (hydroxymethyl) aminomethane hydrochloride (Tris-HCl) buffer, after incubation was completed, the electrode was rinsed with Phosphate Buffer (PBS), thus successfully constructing the PEC sensor.
Further defined, the sequence of the cDNA is: 5' -Biotin-AAACCCGTCAACCACTCTTGAGTGCAGGGGGGTTAATCTTT-C6-NH 2 -3'。
Further defined, the sequence of the aptamer is: 5'-GGGACGTGAGACACAGACCTTCTGCCCTTT-3'.
Further defined, the PEC sensor prepared was used to detect VEGF165.
The invention has the following beneficial effects:
the invention prepares a ligand structure and applies the ligand structure to the synthesis of novel metal organic framework materials, the MOF materials can be used as raw materials for preparing PEC sensors, and the PEC sensors prepared by testing the metal organic framework materials have higher selectivity and high sensitivity to the detection of VEGF165, and the linear range is 10-1 multiplied by 10 8 fM, the lowest detection limit is 0.18. 0.18 fM. Moreover, the response current values of the alpha-fetoprotein (AFP) and carcinoembryonic antigen (CEA) two interfering substances only slightly change, so that the sensitivity of the metal organic framework material is the highest in the related report of VEGF165 detectionPEC sensor materials with the best immunity to interference. In addition, the metal organic framework material synthesis method provided by the invention has the advantages of simple process, mild conditions and the like.
Drawings
FIG. 1 is a synthetic route for preparing ligands for metal organic framework materials;
FIG. 2 is a diagram of intermediate 1 prepared in example 1 1 H-NMR spectrum;
FIG. 3 is a diagram of intermediate 1 prepared in example 1 13 C-NMR spectrum;
FIG. 4 is a mass spectrum of intermediate 1 prepared in example 1;
FIG. 5 is a diagram of intermediate 2 prepared in example 1 1 H-NMR spectrum;
FIG. 6 is a diagram of intermediate 2 prepared in example 1 13 C-NMR spectrum;
FIG. 7 is a mass spectrum of intermediate 2 prepared in example 1;
FIG. 8 shows the ligand prepared in example 1 1 H-NMR spectrum;
FIG. 9 is a diagram of the ligands prepared in example 1 13 C-NMR spectrum;
FIG. 10 is a mass spectrum of the ligand prepared in example 1;
FIG. 11 is a representation of the X-ray structure of metal organic framework material MOF-ET21 prepared in example 1;
FIG. 12 is a graph of the results of selective testing of PEC sensors prepared in example 1 for different substances;
FIG. 13 is a graph of the photocurrent response test results of the PEC sensor prepared in example 1 for different concentrations of VEGF 165;
FIG. 14 is a calibration curve of the PEC sensor prepared in example 1 versus VEGF165 measurement.
Detailed Description
The present invention will be described in further detail with reference to the drawings and examples, in order to make the objects, technical solutions and advantages of the present invention more apparent. It should be understood that the specific embodiments described herein are for purposes of illustration only and are not intended to limit the scope of the invention. The following description of the embodiments of the present invention will be made apparent and fully in view of the accompanying drawings, in which some, but not all embodiments of the invention are shown. All other embodiments, which can be made by those skilled in the art based on the embodiments of the invention without making any inventive effort, are intended to be within the scope of the invention.
In addition, the technical features of the different embodiments of the present invention described below may be combined with each other as long as they do not collide with each other.
The experimental methods used in the following examples are conventional methods unless otherwise specified. The materials, reagents, methods and apparatus used, without any particular description, are those conventional in the art and are commercially available to those skilled in the art.
The sequences of the cDNAs used in the following examples were: 5' -Biotin-AAACCCGTCAACCACTCTTGAGTGCAGGGGGGTTAATCTTT-C6-NH 2 -3'; the sequence of the aptamer is: 5'-GGGACGTGAGACACAGACCTTCTGCCCTTT-3'.
The elemental analysis of the following examples was performed using a german Elementar UNICUBE elemental analyzer.
Example 1:
the process for preparing the metal organic framework material MOF-ET21 in this example is as follows:
(1) As shown in fig. 1, the ligand was synthesized:
(1) synthetic intermediate 1:
to a three-necked flask was added 4-formylphenylboronic acid (7.67 g,51.15 mmol, starting material 2 CAS: 87199-17-5), potassium carbonate (19.67 g,142 mmol) and tetrakis (triphenylphosphine) palladium (1.34 g,1.16 mmol), followed by addition of 151 mL of N, N-dimethylformamide and 2-amino-4-bromobenzoic acid methyl ester (10.7 g,46.5 mmol, starting material 1 CAS: 135484-83-2) under nitrogen protection, the resulting mixture was heated and stirred at 80℃for reaction 20 h, after the reaction was completed, the reaction mixture was slowly cooled to 25℃and extracted with dichloromethane and water, and the obtained organic phase was dried over magnesium sulfate, followed by silica gel column chromatography using N-hexane/dichloromethane (volume ratio 3:7) as eluent to obtain 12.01 g of brown solid, namely intermediate 1, in 92% yield.
The intermediate 1 obtained was structurally characterized:
<1> nuclear magnetic characterization results:
hydrogen spectrum: 1 H NMR (400 MHz, CDCl 3 ):δ9.94 (s, 1H), 8.01 (d, 2H), 7.96 (s, 1H), 7.86 (d, 2H), 7.25 (d, 1H), 6.98 (d, 1H), 4.00 (s, 3H), 3.83 (s, 2H), as shown in fig. 2.
Carbon spectrum: 13 C NMR (100 MHz, CDCl 3 ):δ191.99, 169.05, 150.35, 144.30, 142.68, 138.48, 131.32, 128.93, 127.10, 118.65, 116.46, 109.87, 52.08 as shown in fig. 3.
<2> mass spectrometry characterization results:
ESI(m/z): [M+H] + theoretical calculation C 15 H 13 NO 3 255.27; actual measurement 256.15. As shown in fig. 4.
<3> elemental analysis test results:
theoretical calculation C 15 H 13 NO 3 C, 70.58, H, 5.13, O, 18.80; actual measurements of C, 71.32, H, 6.01, O, 19.65.
In summary, the structure of the intermediate 1 obtained is as follows:
。
(2) synthesis of intermediate 2:
intermediate 1 (3.06 g,12 mmol) was dissolved in 100 mL propionic acid, the resulting reaction mixture was degassed with nitrogen for 20 min, then heated and stirred at 25 ℃ and gradually warmed to 130 ℃, the incubation was performed for 6h, after the reaction was completed, 3, 4-diethylpyrrole (1.48 mg,12 mmol, starting material 3 cas: 16200-52-5) and 2 mL propionic acid were added and the reaction was stirred in the dark for 12 h. After the reaction, the reaction solution was slowly cooled to 25 ℃, the red solid was collected by filtration, and the crude product was purified by silica gel column chromatography using dichloromethane as eluent to obtain 1.19. 1.19 g solid, intermediate 2, in 26% yield.
The intermediate 2 obtained was structurally characterized:
<1> nuclear magnetic characterization results:
hydrogen spectrum: 1 H NMR (400 MHz, CDCl 3 ):δ8.72 (s, 1H), 8.21 (s, 1H), 8.02 (m, 4H), 7.63 (m, 16H), 7.21 (m, 4H), 7.02 (m, 4H), 4.02 (s, 12H), 3.80 (s, 8H), 2.69 (s, 8H), 2.06 (m, 8H), 1.26 (m, 6H), 1.18 (m, 18H), as shown in fig. 5.
Carbon spectrum: 13 C NMR (100 MHz, CDCl 3 ):δ169.05, 165.08, 156.58, 150.35, 146.39, 144.30, 140.46, 138.36, 138.15, 136.85, 136.35, 135.84, 132.97, 128.89, 127.70, 127.10, 118.65, 116.46, 113.87, 112.09, 109.87, 52.08, 18.58, 18.54, 14.62, 14.21 as shown in fig. 6.
<2> mass spectrometry characterization results:
ESI(m/z): [M+H] + theoretical calculation C 92 H 90 N 8 O 8 1435.78; actual measurement 1436.67. As shown in fig. 7.
<3> elemental analysis test results:
theoretical calculation C 92 H 90 N 8 O 8 C, 76.96, H, 6.32, O, 8.91; actual measurements C, 77.85, H, 7.23, O, 9.77.
In summary, the structure of the intermediate 2 obtained is as follows:
。
(3) synthesizing a ligand:
intermediate 2 (0.43 g,0.3 mmol) was dissolved in a mixed solvent of 120 mL tetrahydrofuran and methanol (volume ratio 2:1), potassium hydroxide (8.0 g,142.9 mmol) and 32: 32 mL water were added thereto, then the reaction mixture was refluxed for 12: 12h, after the reaction was completed, the reaction solution was cooled to 25 ℃, the organic solvent was removed by rotary evaporation, the resulting reaction mixture was diluted with 50: 50 mL water, acidified with acetic acid to pH 4, the purple solid was collected by filtration, then washed with water 3 times, each time 100: 100 mL, and finally the purple solid was dried in vacuo to give 0.26: 0.26 g solid as a ligand in 62% yield.
Structural characterization of the ligand obtained:
<1> nuclear magnetic characterization results:
hydrogen spectrum: 1 H NMR (400 MHz, DMSO):δ8.26 (m, 4H), 7.68 (m, 8H), 7.61 (m, 8H), 7.35 (m, 4H), 7.21 (m, 4H), 5.25 (s, 8H), 2.55 (m, 8H), 1.97 (m, 8H), 1.17 (m, 6H), 1.11 (m, 6H), 1.04 (m, 12H), as shown in FIG. 8.
Carbon spectrum: 13 C NMR (100 MHz, DMSO):δ170.77 165.08, 156.58, 147.22, 146.39, 143.96, 140.46, 138.36, 138.15, 136.85, 136.35, 135.84, 132.97, 128.89, 128.04, 127.70, 118.98, 114.25, 113.87, 112.09, 111.84, 18.56, 14.62, 14.21 as shown in fig. 9.
<2> mass spectrometry characterization results:
ESI(m/z): [M+H] + theoretical calculation C 88 H 82 N 8 O 8 1379.67; actual measurement 1380.59. As shown in fig. 10.
<3> elemental analysis test results:
theoretical calculation C 88 H 82 N 8 O 8 C, 76.61, H, 5.99, O, 9.28; actual measurements of C, 77.57, H, 6.77, O, 9.97.
In summary, the structure of the ligand obtained is as follows:
。
(2) Synthetic metal organic framework material MOF-ET21:
the ligand (0.26 g,0.30 mmol) was dissolved in a mixture of 30 mL of N, N-dimethylformamide, 8 mL ethanol and 14. Mu.L of triethylamine, then the reaction mixture was heated to 120℃and 10 mL of N, N-dimethylformamide containing neodymium chloride pentahydrate (0.27 g,0.62 mmol) was added thereto. The mixture was then stirred for reaction 2h to give black nanoparticles. The black nanoparticles were dispersed in 20 mL of N-methylpyrrolidone and anthracene (0.1 g,0.56 mmol) for intercalation, and finally sonicated at 4h to successfully prepare MOF-ET21.
The obtained MOF-ET21 is structurally characterized:
<1> the synthesized MOF-ET21 crystals were stored in glass capillaries and tested for crystal structure using single crystal X-rays, the instrument was a Bruker-Apex type ii CCD detector, and were acquired using a Cu ka (λ= 1.54178 a) X-ray source. The data are that the SADABS program corrects for absorption, and not extinction or decay. The test results are shown in FIG. 11, which are directly solved using the SHELXTL software package.
The PEC sensor is prepared by using the metal organic framework material MOF-ET21, and the specific preparation process is as follows:
the cDNA (50. Mu.L, 20. Mu.M) and the aptamer (50. Mu.L, 20. Mu.M) were diluted to 2. Mu.M and stored at 90℃for 5 min. Then, gradually cooled to 37 ℃. Finally, the mixture was incubated at 37 ℃ for 2h to form dsDNA. Then sequentially placing the Glassy Carbon Electrode (GCE) (5 cm multiplied by 0.4 cm) into acetone, ethanol and pure water, ultrasonically cleaning for 15 min, and then drying by nitrogen; the GCE electrode was then secured with a fluorinated sealing tape (effective area 0.16 cm 2 ) The method comprises the steps of carrying out a first treatment on the surface of the mu.L of MOF-ET21 dispersion (0.75. 0.75 mg ‧ mL -1 ) Drop-coating onto GCE electrode surface, drying 5. 5 h in an electrically heated incubator at 37deg.C, and mixing 10. Mu.L of 1-ethyl-3- (3-dimethylaminopropyl) -carbodiimide/N-hydroxysuccinimide (EDC/NHS) solution (10 mg ‧ mL) -1 /20 mg‧mL -1 ) Drop coated onto MOF-ET21/GCE and activated at 25℃for 2 h. After NSH/EDC activation, 10. Mu.L of dsDNA was coated on MOF-ET21
on/GCE, the carboxyl groups of MOF-ET21/GCE reacted with the amino groups of dsDNA to form dsDNA/MOF-ET21/GCE, incubated at 25℃for 20 min. The dsDNA/MOF-ET21/GCE was then immersed in 0.25 wt% Bovine Serum Albumin (BSA) for 25 min to give the dsDNA/BSA/MOF-ET21/GCE structure. Alkaline phosphatase (ALP) (8. Mu.L, 0.5. 0.5 mg ‧ mL) −1 ) Added to the surface of dsDNA/BSA/MOF-ET21/GCE, and placed at 4℃for 2h, ALP-dsDNA/BSA/MOF-ET21/GCE was obtained by the biotin-streptavidin system. Finally, ALP-dsDNA/BSA/MOF-ET21/GCE was added to a solution containing 3 mmoL/L Tris (hydroxymethyl) aminomethane hydrochloride (Tris-HCl) buffer, after incubation, the electrode was rinsed with Phosphate Buffer (PBS), i.e. the PEC sensor was successfully constructed.
The performance of the PEC sensor obtained was tested, the test procedure and results were as follows:
first, test for VEGF165 selectivity
The three substances, VEGF165 of 10 fM, AFP of 10 fM, CEA of 10 fM, were selectively tested using PEC sensors using alpha-fetoprotein (AFP) and carcinoembryonic antigen (CEA) as potential interferents.
The test results are shown in fig. 12, with PEC sensors exhibiting significant photocurrent response only in the presence of VEGF165. The change in photocurrent was only slight for both alpha-fetoprotein (AFP) and carcinoembryonic antigen (CEA) interferons. The results indicate that PEC sensors have higher selectivity for detection of VEGF165.
Second, photocurrent response test to different concentrations of VEGF165
At a bias voltage of 0.1V, 10 fM,100 fM,1×10 pairs of PEC sensors are utilized 3 fM，1×10 4 fM，1×10 5 fM，1×10 6 fM，1×10 7 fM，1×10 8 Photo current response tests were performed with different concentrations of fM VEGF165.
The test results are shown in FIG. 13, where as the concentration of VEGF165 increases, more VEGF165 separates from the sensing interface, the charge transfer resistance decreases, promoting separation of photogenerated electron-hole pairs, and the PEC signal increases with concentration at 10-1×10 8 The fM increases in range and gradually increases.
In addition, the ratio of 10 to 1×10 8 VEGF165 (deltaI=I-I 0 ) The change in photocurrent before and after the specific recognition is linearly related to the logarithm of the concentration thereof, as shown in fig. 14, the formula of the linear relationship is as follows: deltaI=0.189lgc VEGF165 -0.038（R 2 =0.998), resulting in a detection limit of 0.18 fM (S/n=3).
It is apparent that the above examples are given by way of illustration only and are not limiting of the embodiments. Other variations or modifications of the above teachings will be apparent to those of ordinary skill in the art. It is not necessary here nor is it exhaustive of all embodiments. While still being apparent from variations or modifications that may be made by those skilled in the art are within the scope of the invention.

Claims (3)

1. A metal organic framework material is characterized in that the material is simply called MOF-ET21 and has a chemical formula of [ Nd (L) ] 2 ]Wherein L is C 88 H 82 N 8 O 8 The method comprises the steps of carrying out a first treatment on the surface of the The ligand structure of the metal organic framework material is as follows:
2. use of the metal-organic framework material of claim 1 for the preparation of PEC sensors.
3. Use of a metal-organic framework material according to claim 2, characterized in that PEC sensors are used for detecting VEGF165.
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Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110156755A (en) * 2019-05-29 2019-08-23 杭州师范大学 Four pyridine phenyl pyrazines and preparation method thereof, application
CN110731961A (en) * 2014-10-14 2020-01-31 芝加哥大学 Metal organic framework, pharmaceutical preparation and use thereof in preparing medicament
CN112521362A (en) * 2020-12-18 2021-03-19 浙江理工大学 Method for synthesizing cyclic carbonate based on functionalized metalloporphyrin/quaternary phosphonium salt dual-catalytic system
CN113318707A (en) * 2021-06-11 2021-08-31 曲阜师范大学 Organic supermolecule gel system of binuclear rhodium-porphyrin derivative and preparation method thereof
CN114160105A (en) * 2021-11-26 2022-03-11 武汉工程大学 High-selectivity boric acid-doped metal organic framework magnetic adsorbent with core-shell structure and preparation method and application thereof
CN116143618A (en) * 2023-04-19 2023-05-23 吉林省卓材新研科技有限公司 Metal organic frame material for water-based zinc ion battery, ligand and application

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110731961A (en) * 2014-10-14 2020-01-31 芝加哥大学 Metal organic framework, pharmaceutical preparation and use thereof in preparing medicament
CN110156755A (en) * 2019-05-29 2019-08-23 杭州师范大学 Four pyridine phenyl pyrazines and preparation method thereof, application
CN112521362A (en) * 2020-12-18 2021-03-19 浙江理工大学 Method for synthesizing cyclic carbonate based on functionalized metalloporphyrin/quaternary phosphonium salt dual-catalytic system
CN113318707A (en) * 2021-06-11 2021-08-31 曲阜师范大学 Organic supermolecule gel system of binuclear rhodium-porphyrin derivative and preparation method thereof
CN114160105A (en) * 2021-11-26 2022-03-11 武汉工程大学 High-selectivity boric acid-doped metal organic framework magnetic adsorbent with core-shell structure and preparation method and application thereof
CN116143618A (en) * 2023-04-19 2023-05-23 吉林省卓材新研科技有限公司 Metal organic frame material for water-based zinc ion battery, ligand and application

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